LymeNet Flash: Help with finding a doctor...

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » Help with finding a doctor...

UBBFriend: Email this page to someone!

Author

Topic: Help with finding a doctor...

Gavintfn
Junior Member
Member # 21431

posted

Ok, so if someone could help me find a doctor, without posting his name, and without me posting my e-mail address, I'd appreciate it.... I had a tick on me almost 2 1/2 weeks ago...About 1 week ago, I noticed a quarter sized red lump, with a white center that seems to filled with puss. ...exactly where the tick was. now today, I started having flu symptoms.achy body, upset stomach, hot flashes, pale skin...Now, Im more than happy to send someone a picture of me, and my bump/ infection looking thing. Doing what ever you would like in the picture to prove that I have what could be a valid case...but after reading this site, It scares me that my doctor might not know how to diagnose this accurately. So, could someone please help me out? Thank you....

By the way, what is all the secrecy about?....It's lime disease, not HIV....I might have it and I don't care who knows, I would tell anyone in hopes of finding a good doctor. I'm not trying to be rude, but for those who would like to stay anonymous, just make up a pseudonym.

Sorry about the rant...I'm just a little on edge because multiple sites do such a good job scaring you about Lyme disease but no one responds to my posts.

--------------------
Gavin

Posts: 4 | From COumbus, ohio | Registered: Jul 2009 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Let me know if you didn't get any names from "iseekids".

As for the secrecy, we are trying to protect our doctors. They are being harrassed and threatened with license removal for treating us.

This is a very political disease, as you'll soon find out.

We're not afraid to say we have lyme.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001 | IP: Logged |

bettyg
Unregistered

posted

this one should be deleted also .... thanks!

you were given names from iseekids in 1st post

i sent you welcome letter and posting guidelines w/links galore of good info

IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/